Interference With Quorum-Sensing Signal Biosynthesis as a Promising Therapeutic Strategy Against Multidrug-Resistant Pathogens

被引:51
作者
Martinez, Osmel Fleitas [1 ,2 ]
Rigueiras, Pietra Orlandi [2 ]
Pires, Allan da Silva [2 ]
Porto, William Farias [2 ,3 ,4 ]
Silva, Osmar Nascimento [3 ]
de la Fuente-Nunez, Cesar [5 ,6 ,7 ,8 ,9 ]
Franco, Octavio Luiz [1 ,2 ,3 ]
机构
[1] Univ Brasilia, Programa Posgrad Patol Mol, Brasilia, DF, Brazil
[2] Univ Catolica Brasilia, Ctr Anal Prote & Bioquim, Brasilia, DF, Brazil
[3] Univ Catolica Dom Bosco, S Inova Biotech, Programa Posgrad Biotecnol, Campo Grande, Brazil
[4] Porto Reports, Brasilia, DF, Brazil
[5] MIT, Synthet Biol Grp, Synthet Biol Ctr, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[6] MIT, Elect Res Lab, Cambridge, MA 02139 USA
[7] MIT, Dept Elect Engn & Comp Sci, Dept Biol Engn, Cambridge, MA 02139 USA
[8] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[9] Ctr Microbiome Informat & Therapeut, Cambridge, MA 02139 USA
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2019年 / 8卷
关键词
virulence; antibiotic resistance; quorum sensing; quorum-sensing inhibition; anti-virulence therapy; S-RIBOSYLHOMOCYSTEINE ANALOGS; METHYLTHIOADENOSINE/S-ADENOSYLHOMOCYSTEINE NUCLEOSIDASE; TRANSITION-STATE STRUCTURE; SMALL-MOLECULE INHIBITORS; PSEUDOMONAS-AERUGINOSA; STAPHYLOCOCCUS-AUREUS; BIOFILM FORMATION; ESCHERICHIA-COLI; 5'-METHYLTHIOADENOSINE/S-ADENOSYLHOMOCYSTEINE NUCLEOSIDASE; CATALYTIC MECHANISM;
D O I
10.3389/fcimb.2018.00444
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Faced with the global health threat of increasing resistance to antibiotics, researchers are exploring interventions that target bacterial virulence factors. Quorum sensing is a particularly attractive target because several bacterial virulence factors are controlled by this mechanism. Furthermore, attacking the quorum-sensing signaling network is less likely to select for resistant strains than using conventional antibiotics. Strategies that focus on the inhibition of quorum-sensing signal production are especially attractive because the enzymes involved are expressed in bacterial cells but are not present in their mammalian counterparts. We review here various approaches that are being taken to interfere with quorum-sensing signal production via the inhibition of autoinducer-2 synthesis, PQS synthesis, peptide autoinducer synthesis, and N-acyl-homoserine lactone synthesis. We expect these approaches will lead to the discovery of new quorum-sensing inhibitors that can help to stem the tide of antibiotic resistance.
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页数:17
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